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Recruiting NCT06933693

Mixed Vs Blocked Search: Four Unique Tasks

No phase Interventional Vision Healthy Attention

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Mixed trials, Blocked Trials.
Who it may be relevant to
Registry conditions: Vision, Healthy, Attention. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Prevalence Effects in Visual Search: Theoretical and Practical Implications

Overview

The goal is to look for qualitative differences in visual search behavior when one search is performed many times in a row compared to when multiple search tasks are intermixed. Four search tasks are tested. In the Mixed condition, the four tasks are randomly changed from trial to trial. In the Blocked condition, each task is run as a block of 100 trials.

Detailed description

NOTE: This registration is linked to a Human Subjects registration in ASSIST. That, in turn, is part of an NCI Grant, R01EY017001. The grant describes many proposed experiments and notes that many others might be done as follow-up studies. At the suggestion of the NIH, the investigators grouped these studies into several "studies", each covering multiple experiments. The experiment described here is part of Aim 1 of R01EY017001. It is not possible to register a set of experiments through the PRS system in CT.gov and it is not possible to file an annual report for the grant (RPPR) without an NCT number for projects that have started collecting participants. Accordingly, the investigators are describing one experiment here that would be part of the "Project 1" bundle of studies.

When scientists study visual search in the lab, they usually ask people to do dozens of instances of the same type of task in a block. (e.g., Please find a vertical line….in the next 100 trials). However, in many (maybe most) visual searches in the real world, the participants are rarely looking for the same item (or same type of item) back-to-back. You do one search. Then the participants do another, and so on. (Find the jam. Now, find the bread. Now find a knife, etc). We want to know if the investigators would get the same results if the investigators mixed different searches together as the investigators do when the investigators test in long blocks of one specific type of search. This is important because the investigators want to know if the rules, established by years of blocked experiments, continue to apply in the more mixed real world.

There are multiple variants of this mixed/block experiment. In Experiment 1, observers are trained on four different search tasks. Then they perform 400 trials in the Mixed condition and the Blocked condition. In the Mixed condition, the four tasks are randomly changed from trial to trial. In the Blocked condition, each task is run as a block of 100 trials. Stimuli are placed in random locations in a jiggled 5 x 5 grid. The grid are placed within square field that is 0.5 of the maximum height of the screen. Each stimulus item fit into an invisible box that is 0.11 of the screen height. If the viewing distance is about 60 cm, a standard computer screen would show a stimulus field of about 15 deg on a side and each item would be placed in a box of about 3 x 3 deg. The background is white. Trials are divided evenly between three set sizes: 8, 16, and 24 items and evenly between target-present and absent trials. Stimuli are presented until the observer responds by pressing either 'p' or 'q' to indicate target present or absent, respectively. Accuracy feedback is provided after each trial.

Interventions

  • Behavioral Mixed trials
    All tasks will be randomly mixed in a single block of 400 trials.
  • Behavioral Blocked Trials
    Each search task will be presented in a block of trials.

Primary outcome measures

  • Response Time (RT) [Time frame: Through study completion, an average of one year]
Secondary outcome measures (1)
  • Accuracy [Time frame: through study completion, an average of one year]

Eligibility criteria

Inclusion criteria

  • Pass Ishihara color vision test

Exclusion criteria

  • vision less than 20/25 with correction
  • history of neuromuscular or visual disorders

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Sequential
Masking
Open label
Primary purpose
Basic science

Study locations

United States · 1 center
  • Brigham & Women's Hospital — Boston

Identifiers

NCT: NCT06933693 · 2007P000646-G · R01EY017001

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗